Forskningskoordinator - Lääkealan turvallisuus- ja kehittämiskeskus Fimea

The position is located within the Clinical Pharmacology unit of the Marketing Authorization department. The unit is responsible for evaluating the efficacy and safety of medicines and processing marketing authorization applications within its scope. The responsibilities of the research coordinator include, where appropriate, writing assessment reports for medicinal products (clinical type IB variation applications and applications for parallel products under section 10(1)), evaluating clinical documentation for renewal applications, assessing product information, and reviewing translations. We conduct recruitment anonymously to promote a uniform and equitable process. We select candidates for interviews without knowledge of their name, age, gender, location (all contact details), native language, nationality, or appearance. Due to anonymous recruitment, we prefer applications primarily in electronic form via valtiolle.fi. Please also avoid including personal data in the open text fields of your application. If you inquire about the position by phone, please avoid sharing information that could compromise anonymity. We do not accept attachments.